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GLP/GCLP Quality Assurance Auditor

Date: Aug 2, 2022

Location: Netanya, IL, 11

Company: Teva Pharmaceuticals

Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

TEVA's Global R&D unit is looking for GLP/GCLP Quality Assurance Auditor, for a challenging role in Abic site in Netanya for.
The position includes Involvement in Non-Clinical and Bioanalytical QA related activities that are planned and performed to assure quality and compliance with global and local procedures, relevant regulations,  through regulated studies, documents and non-clinical sites.
•    Participate in conduct GLP site audits
•    Participate in conduct of study protocol audit, amendments, raw data and reports and other audits in the support of a GLP/GCLP studies.

•    Participate in conduct of process and study based audits at a GLP/GCLP Laboratory in support of regulated studies. 
•    Participate in conduct of facility prequalification/qualification audits at Contract Research Organizations (CROs).
•    To issue QA Audit Reports for the different audit activities
•    To participate in SOPs, work instructions, forms and templates development and review
•    Participate in review of non-clinical parts of regulatory submissions (e.g. INDs, IBs). 
•    Support GLP training activities 
•    Support inspection readiness activites
 

Temporary position replacement for maternity leave

Qualifications

•    Life Sciences background at least Bsc. level.
•    Experience as an auditor - An advantage
•    Professional experience in laboratory work specializing in biological experiments, Bioassays, or GLP research facility
•    Ability to work independently as well as to effectively communicate and collaborate in a team environment
•    Extensive experience with computer software usages
•    Fluent English- Must

Function

Quality

Sub Function

R&D Quality

Reports To

Senior Director GLP/GCLP Quality, Global QA

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.